结果酶切和测序证实PTEN基因克隆和真核表达载体构建成功。
Results Restriction enzyme analysis and DNA sequence analysis showed that PTEN gene was cloned and the eukaryotic expression vector was constructed successfully.
本文简要介绍了近年来在植物表达载体构建方面所采用的一些新策略，这些策略有助于增强外源基因的表达水平、提高生物工程体的安全性。
This article reviews the new strategies currently used in construction of plant expression vector for plant genetic engineering. These strategies are important for obtaining better expression of fo...
本研究旨在构建具有猪 MSTN 前肽基因定点突变的真核表达载体。
This research intended to construct a eukaryotic expression vector with a site-directed mutation of porcine MSTN propeptide gene.
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